Substituted isoquinolines, isochromanones and isothiochromanones that inhibit the pro-inflammatory cytokines tumor necrosis factor-alpha (TNF-alpha) and/or interleukin-6 (IL-6) and/or the enzyme cyclooxygenase-2 (COX-2) and/or interleukin-10 (IL-10). Compositions containing such compounds and methods of using such compounds for treatment and/or prevention of inflammation, inflammatory diseases, immunologic diseases and other diseases mediated by TNF-alpha, IL-6, COX-2 and/or IL-10 are also disclosed.
抑制促炎细胞因子肿瘤坏死因子-α(TNF-α)和/或白细胞介素-6(IL-6)和/或环
氧合酶-2(COX-2)和/或白细胞介素-10(I
L-10)的取代
异喹啉酮、异
色酮和异
硫色酮。还公开了含有此类化合物的组合物和使用此类化合物治疗和/或预防炎症、炎症性疾病、免疫性疾病和 TNF-α、IL-6、COX-2 和/或 I
L-10 介导的其他疾病的方法。